# Systematic review of prophylactic antibacterial agents for radiation-induced oral mucositis in head and neck cancer

**Authors:** Daniel S. Alicea, Mark Han, Zahidul Islam, Rachel Schwartz, Thomas J. Ow, Vikas Mehta, Madhur Garg, Beth N. McLellan, Rafi Kabarriti

PMC · DOI: 10.1007/s00520-026-10439-x · Supportive Care in Cancer · 2026-02-23

## TL;DR

This systematic review examines whether antibacterial agents can prevent or reduce mouth sores caused by radiation in head and neck cancer patients.

## Contribution

The study provides a comprehensive analysis of antibacterial prophylaxis for radiation-induced oral mucositis, highlighting inconsistencies and the potential of Nigella sativa.

## Key findings

- Evidence for povidone iodine, PTA, and SAMITAL was inconclusive or showed no significant reduction in mucositis severity.
- Nigella sativa showed potential in reducing mucositis incidence and severity compared to standard care.
- Patient-reported outcomes sometimes showed improvement despite no change in clinician-assessed scores.

## Abstract

To examine the use of treatments with antibacterial properties as prophylaxis prior to radiotherapy (RT), either alone or in combination with chemotherapy (CT), to prevent and reduce radiation-induced oral mucositis (RIOM) in patients with head and neck cancer (HNC).

A systematic search following PRISMA guidelines was conducted across PubMed, Embase, Web of Science, and the Cochrane Library to identify relevant studies published in English through March 2025.

Eligible studies assessed prophylactic antibacterial interventions aimed at preventing RIOM.

From 86 retrieved citations, 9 articles met inclusion criteria. Antibacterial agents assessed included polymyxin, tobramycin, amphotericin (PTA), povidone iodine, SAMITAL, and Nigella sativa (NS). Evidence supporting povidone iodine, PTA, and SAMITAL was inconclusive or failed to demonstrate statistically significant reductions in RIOM severity. Several studies reported discordant findings, with statistically significant improvements in patient-reported symptoms or quality-of-life measures despite nonsignificant clinician-assessed scores. NS demonstrated potential benefits in reducing RIOM incidence and severity compared with standard of care and other antibacterial agents.

The systematic review highlights limited and inconsistent evidence supporting antibacterial prophylaxis for preventing and reducing RIOM severity in patients with HNC undergoing RT. Discrepancies between patient-reported outcomes and clinical-assessed grading suggest some treatments may provide symptomatic benefit not captured by traditional scoring systems. NS mouthwashes showed preliminary promise; however, evidence remains insufficient to establish superiority, and safety and regulatory concerns are persistent, particularly in immunosuppressed patients. Given the role of bacterial colonization and microbial dysbiosis in RIOM pathogenesis, larger, well-designed clinical trials with rigorous safety evaluations are warranted to investigate bacterial-directed preventive therapies.

## Linked entities

- **Chemicals:** tobramycin (PubChem CID 36294), amphotericin (PubChem CID 5280965), povidone iodine (PubChem CID 410087)
- **Diseases:** head and neck cancer (MONDO:0005627)

## Full-text entities

- **Genes:** IL6 (interleukin 6) [NCBI Gene 3569] {aka BSF-2, BSF2, CDF, HGF, HSF, IFN-beta-2}, IL1A (interleukin 1 alpha) [NCBI Gene 3552] {aka IL-1 alpha, IL-1A, IL1, IL1-ALPHA, IL1F1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}
- **Diseases:** Cancer (MESH:D009369), dysbiosis (MESH:D064806), bacteremia (MESH:D016470), atrophy (MESH:D001284), Oral Mucositis (MESH:D013280), ulcerated mucosa (MESH:D014456), edema (MESH:D004487), toxicities (MESH:D064420), weight loss (MESH:D015431), HNC (MESH:D006258), dysphagia (MESH:D003680), inflammation (MESH:D007249), skin diseases (MESH:D012871), malnutrition (MESH:D044342), pain (MESH:D010146), erythema (MESH:D004890), nasopharyngeal cancer (MESH:D009303), RIOM (MESH:D007953), HNSCC (MESH:D000077195), superinfections (MESH:D015163), Mucositis (MESH:D052016), bleeding (MESH:D006470), ARD (MESH:D054508), BD (MESH:D001424), radiation induced mucositis (MESH:D009381), dysarthria (MESH:D004401)
- **Chemicals:** Mupirocin (MESH:D016712), Amphotericin (MESH:D000666), benzydamine hydrochloride (MESH:D001591), BD (-), thymoquinone (MESH:C003466), SA (MESH:D000077145), chlorhexidine (MESH:D002710), Tobramycin (MESH:D014031), reactive oxygen species (MESH:D017382), Povidone iodine (MESH:D011206), polyene (MESH:D011090), water (MESH:D014867), chlorhexidine gluconate (MESH:C010882), IS (MESH:D007455)
- **Species:** Bacteria Latreille et al. 1825 (Bacteria stick insect, genus) [taxon 629395], Staphylococcus aureus (species) [taxon 1280], Homo sapiens (human, species) [taxon 9606], Candida [taxon 1535326], Saccharomyces cerevisiae (baker's yeast, species) [taxon 4932], Vaccinium myrtillus (bilberry, species) [taxon 180763], Nigella sativa (black-caraway, species) [taxon 555479]

## Full text

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Source: https://tomesphere.com/paper/PMC12929255